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Nosiboo PRO Blue

FDA UDI

Class II (US FDA UDI)

by ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag

Identity

Trade Name
Nosiboo PRO Blue FDA UDI
Generic Name
Nasal aspirator, electric FDA UDI
Device Name
Nosiboo Pro, USA, blue, Electric nasal aspirator FDA UDI
Model / Reference
NO-05-01 FDA UDI
Description
Nosiboo Pro, USA, blue, Electric nasal aspirator FDA UDI

Identifiers

Catalog Number
NO-05-01 FDA UDI
Primary DI / UDI-DI
05999885976928 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Nasal aspirator, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal aspirator, electricNasal aspirator, vacuum

Nosiboo PRO Blue by ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal aspirator, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4e2bba14-8f33-457a-bd21-9d47a32a3b42 35 fields · synced Jun 1, 2026